Examples of 'preparation of example' in a sentence
Meaning of "preparation of example"
Preparation of example is the act of creating or setting up a sample or instance to illustrate or explain something
How to use "preparation of example" in a sentence
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preparation of example
Preparation of Example BMa and BMb Examples BMa and BMb.
This compound can be used as such for the preparation of example 1.
EXAMPLES Preparation of example embodiments of the invention.
Scheme 2 below is an illustration of an alternative method used for the preparation of example 1.
The preparation of example 1 is detailed below.
The same catalytic emulsion preparation of Example 3 was used.
Therefore, the preparation of Example 7 is a good preparation satisfying the above criteria.
This compound was used for the preparation of Example 2.
The purified enzymatic preparation of Example 2 is used to prepare a hypoallergenic infant formula.
This product is deprotected according to the method described in the preparation of Example 1from 1D.
Thus the lyophilized preparation of Example 2 was obtained.
The following Example was prepared using the procedures outlined for the preparation of Example 1.
The intermediates required for the preparation of Example 64 were prepared as follows.
Then the preparation of Example 27 is cast on the top with a knife over roll system.
The procedure described for the preparation of Example 4 was used.
See also
Preparation of Example 1 is representative of the chemistry described in Scheme 3.
An alternative method useful for the preparation of Example 1 is described below.
Preparation of Example 2 Example 2 was prepared using the following synthetic sequence.
The overall synthesis for the preparation of Example 1 is shown below.
The effect was however much inferior to the effect observed using the preparation of Example 4.
According to the method of preparation of Example 2 one can also prepare granules.
Prepared from Compound B by the procedure analogous to the preparation of Example 27.
A single treatment with the preparation of Example 1 was administered one week later.
This compound was formed as a byproduct during preparation of Example 247b.
Example 2, Method of preparation of example chocolates or compound chocolate products of the invention.
Reaction scheme 4 depicts the preparation of example 1.
The preparation of example 1 is repeated, using an amount of retinoic acid of 5 g.
In the same manner as stated for the preparation of Example 5 the following are prepared,.
The preparation of Example 1 is reproduced, with the exceptions that,.
General procedure for preparation of Example 3.
In the preparation of Example 8, there was a mild exotherm.
This method was used for the preparation of example 36.
Example B g of a preparation of example 1 are mixed with 50 g of lactose and 8 g of xanthan.
This compound was synthesized according to a procedure for the preparation of example 69, using n - butyl bromide.
The bioadhesive preparation of Example 26 is directly casted on the film of Example 25 and dried.
Formylurea was used for the preparation of Example 27.
Preparation of Example 4 Example 4 is prepared from Example 1 by the following reaction.
The aryl fluoride used in the preparation of Example 12a was prepared as described below.
Figure 12 is a schematic showing a procedure for the preparation of Example 1.
Fig . 2b shows the food preparation of Example 2a after oven cooking.
This oil was utilized without purification for the preparation of Example 38b.
Example 2 The a-amylase preparation of Example 1 was coated by means of spray chilling.
The resulting material was de-benzylated as described above for the preparation of Example 60.
This acylacion method was used for the preparation of example 8, using INT 6D as starting material.
De-benzylation and hydrolysis proceeded as described above for the preparation of Example 60.
Preparation of Example 3 Example 3 was prepared from Example 1 by the following synthetic reaction.
Fig . 1 shows a photograph of the injectable preparation of Example 1 immediately after production.
Compound 61B was converted to the title compound in a manner similar to the preparation of Example 1.
The preparation of Example I was repeated up to and including an aftertreatment at 60°C for 3 hours.
Prepared using a procedure similar to that used in the preparation of Example 643.
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